The Predisposition for Type 2 Diabetes Mellitus and Metabolic Syndrome

Author:

Zenoaga-Barbăroșie C1,Berca L2,Vassu-Dimov T1,Toma M3,Nica MI4,Alexiu-Toma OA1,Ciornei C56,Albu A6,Nica S67,Nistor C58,Nica R910

Affiliation:

1. Department of Genetics , University of Bucharest , Bucharest , Romania

2. Molecular Biology Department , National Research and Development Institute for Food Bioresources – IBA Bucharest , Bucharest , Romania

3. Emergency Department , Central Military Emergency Hospital Dr. Carol Davila , Bucharest , Romania

4. University of Medicine and Pharmacy Carol Davila , Bucharest , Romania

5. Preclinical Department , University of Medicine and Pharmacy Carol Davila , Bucharest , Romania

6. Emergency Department , Bucharest Emergency University Hospital , Bucharest , Romania .

7. Clinic Department 4 , University of Medicine and Pharmacy Carol Davila , Bucharest , Romania

8. Thoracic Surgery , Central Military Emergency Hospital Dr. Carol Davila , Bucharest , Romania

9. Surgery 2, Central Military Emergency Hospital Dr. Carol Davila , Bucharest , Romania

10. Special Disciplines , University of Medicine and Pharmacy Carol Davila , Bucharest , Romania

Abstract

Abstract Type 2 diabetes mellitus (T2DM) and metabolic syndrome (MetS) are diseases caused by the interaction of genetic and non-genetic factors. Therefore, the aim of our study was to investigate the association between six common genetic polymorphisms and T2DM and MetS in males. A total of 120 T2DM, 75 MetS, and 120 healthy controls (HC) were included in the study. ACE ID, eNOS 4a/b, ATR1 A1166C, OXTR (A>G), SOD1 +35A/C, CAT-21A/T gene polymorphisms were genotyped by PCR or PCR-RFLP techniques. T2DM was diagnosed at an earlier age compared to MetS (54 vs 55 years old, p=0.0003) and the difference was greater in carriers of the OXTR G allele (54 vs 56 years old, p=0.0002) or both OXTR G and eNOS b alleles (54 vs 56, p=0.00016). The SOD1 AA genotype (O.R.=0.11, p=0.0006) and the presence of both ACE I and OXTR1 A (O.R.=0.39, p=0.0005) alleles revealed to be protective for T2DM. SOD1 AA and AC genotypes were protective factors for triglyceride (p=0.0002 and p=0.0005, respectively) and HDL cholesterol (p=0.0002 and p=0.0004, respectively) levels in T2DM patients. ACE DD was identified more frequently in hypertensive T2DM patients (O.R.=3.77, p=0.0005) and in those who reported drinking alcohol (p=0.0001) comparing to HC and T2DM patients who did not drink alcohol, respectively. We observed that T2DM patients who reported drinking alcohol had an increased frequency of ACE DD and eNOS bb (p<0.0001), or ACE DD and OXTR G (p<0.0001) compared to non-drinkers. No gene polymorphisms were associated with MetS.

Publisher

Walter de Gruyter GmbH

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